Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 16
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs374052197
PDPN
0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs745934102
PDPN
0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1320938886
BLZF1
0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs1249080185
EPHB2
0.882 0.080 1 22784698 missense variant G/A snv 3
rs751859698
MSH4
0.925 0.040 1 75898031 missense variant T/A;C snv 1.2E-05 2